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1.
J Plast Reconstr Aesthet Surg ; 74(12): 3213-3234, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34489212

RESUMO

BACKGROUND: Auricular reconstruction for microtia is most frequently performed using autologous costal cartilage (ACC) or porous polyethylene (PPE) implants. Short-term results are generally promising, but long-term results remain unclear. Long-term outcomes were explored in this systematic review, and minimal reporting criteria were suggested for future original data studies. METHODS: A systematic literature search was conducted in MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials from inception through October 14, 2020. Articles on auricular reconstruction in patients with microtia using ACC or PPE were included if postsurgical follow-up was at least 1 year. Outcome reporting was split into separate publications, and results on complications were reported previously. This publication focused on long-term aesthetic, patient-reported, and sensitivity outcomes. RESULTS: Forty-one publications reported on these outcomes. Both materials led to aesthetically pleasing results and high rates of patient satisfaction. ACC frameworks grew similarly to contralateral ears, and the anterior surface of auricles regained sensitivity. Furthermore, postoperative health-related quality of life (HRQoL) outcomes were generally good. Data synthesis was limited due to considerable variability between studies and poor study quality. No conclusions could be drawn on the superiority of either method due to the lack of comparative analyses. CONCLUSION: Future studies should minimally report (1) surgical efficacy measured using the tool provided in the UK Care Standards for the Management of Patients with Microtia and Atresia; (2) complications including framework extrusion or exposure, graft loss, framework resorption, wire exposure and scalp/auricular scar complications and (3) HRQoL before and after treatment using the EAR-Q patient-reported outcome measure (PROM).


Assuntos
Microtia Congênita/cirurgia , Estética , Medidas de Resultados Relatados pelo Paciente , Procedimentos de Cirurgia Plástica/métodos , Cartilagem Costal/transplante , Humanos , Satisfação do Paciente , Complicações Pós-Operatórias , Próteses e Implantes
2.
J Plast Reconstr Aesthet Surg ; 74(12): 3235-3250, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34481742

RESUMO

BACKGROUND: Microtia is a rare disorder characterized by malformation or even complete absence of the auricle. Reconstruction is often performed using autologous costal cartilage (ACC) or porous polyethylene implants (PPE). However, the long-term outcomes of both methods are unclear. OBJECTIVE: This systematic review aimed to analyze long-term complications and suggest minimal reporting criteria for future original data studies. METHODS: A systematic literature search was conducted in MEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials from inception through October 14, 2020. Articles on auricular reconstruction in patients with microtia using ACC or PPE were included provided that the follow-up period was at least one year. This publication focused on long-term complications reported in patients with a postoperative follow-up period of at least one year. RESULTS: Twenty-nine publications reported on complications during long-term follow-up. Overall long-term complication rates were not reported. The incidence of individual complications during long-term follow-up was less than 10% after ACC reconstruction and less than 15% in PPE reconstruction. Framework resorption and wire exposure were reported even after an extended follow-up of more than five years after ACC reconstruction, while reports on the extended long-term results of PPE reconstruction are limited. Data synthesis was limited due to heterogeneity and poor study quality. CONCLUSIONS: Future studies should report on long-term complications including framework exposure or extrusion, graft loss, framework resorption, wire exposure and scalp and auricular scar complications. We recommend a surgical follow-up of at least five years.


Assuntos
Microtia Congênita/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Complicações Pós-Operatórias , Cartilagem Costal/transplante , Humanos , Próteses e Implantes
4.
Br J Dermatol ; 182(2): 434-443, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31111470

RESUMO

BACKGROUND: Genotype-phenotype studies can identify subgroups of patients with specific clinical features or differing outcomes, which can help shape management. OBJECTIVES: To characterize the frequency of different causative genotypes in congenital melanocytic naevi (CMN), and to investigate genotype-phenotype and genotype-outcome associations. METHODS: We conducted a large cohort study in which we undertook MC1R genotyping from blood, and high-sensitivity genotyping of NRAS and BRAF hotspots in 156 naevus biopsies from 134 patients with CMN [male 40%; multiple CMN 76%; projected adult size (PAS) > 20 cm, 59%]. RESULTS: Mosaic NRAS mutations were detected in 68%, mutually exclusive with BRAF mutations in 7%, with double wild-type in 25%. Two separate naevi were sequenced in five of seven patients with BRAF mutations, confirming clonality. Five of seven patients with BRAF mutations had a dramatic multinodular phenotype, with characteristic histology distinct from classical proliferative nodules. NRAS mutation was the commonest in all sizes of CMN, but was particularly common in naevi with PAS > 60 cm, implying more tolerance to that mutation early in embryogenesis. Facial features were less common in double wild-type patients. Importantly, the incidence of congenital neurological disease, and apparently of melanoma, was not altered by genotype; no cases of melanoma were seen in BRAF-mutant multiple CMN, however, this genotype is rare. CONCLUSIONS: CMN of all sizes are most commonly caused by mutations in NRAS. BRAF is confirmed as a much rarer cause of multiple CMN, and appears to be commonly associated with a multinodular phenotype. Genotype in this cohort was not associated with differences in incidence of neurological disease in childhood. However, genotyping should be undertaken in suspected melanoma, for guidance of treatment. What's already known about this topic? Multiple congenital melanocytic naevi (CMN) have been shown to be caused by NRAS mosaic mutations in 70-80% of cases, by BRAF mosaicism in one case report and by inference in some previous cases. There has been debate about genotypic association with different sizes of CMN, and no data on genotype-outcome. What does this study add? NRAS mosaicism was found in 68%, BRAF in 7% and double wild-type in 25% of cases of CMN. NRAS was the commonest mutation in all sizes of CMN, but was nearly universal in projected adult size > 60 cm. BRAF is often associated with a distinct multinodular clinical/histological phenotype. Adverse outcomes did not differ between genotypes on current numbers.


Assuntos
Nevo Pigmentado , Neoplasias Cutâneas , Adulto , Estudos de Coortes , Genótipo , Humanos , Masculino , Mutação/genética , Nevo Pigmentado/genética , Fenótipo , Proteínas Proto-Oncogênicas B-raf/genética , Neoplasias Cutâneas/genética
7.
Int J Oral Maxillofac Surg ; 46(10): 1330-1337, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28641899

RESUMO

A retrospective cohort study was set up to analyse the prevalence and treatment of obstructive sleep apnoea (OSA) in relation to the severity of the deformity in patients with craniofacial microsomia (CFM). This study included a population of 755 patients with CFM from three craniofacial centres. Medical charts were reviewed for severity of the deformity, types of breathing difficulty, age at which breathing difficulty first presented, treatment for OSA, and treatment outcome. In total, 133 patients (17.6%) were diagnosed with OSA. Patients with Pruzansky IIB/III classification or bilateral craniofacial microsomia were significantly more often diagnosed with OSA than unilaterally affected patients of Pruzansky I/IIA classification. The initial treatment of OSA consisted of adenotonsillectomy, tracheotomy, or non-invasive positive pressure ventilation. Thirty-seven patients received more than one treatment (range 1-3). In this study, the prevalence of OSA in patients with CFM was higher than the prevalence in the healthy population described in the literature. Although several treatment modalities are available for the treatment of OSA in patients with CFM, treatment should be individualized and based on clinical symptoms, the severity of the deformity, and comorbidities.


Assuntos
Síndrome de Goldenhar/complicações , Apneia Obstrutiva do Sono/etiologia , Apneia Obstrutiva do Sono/terapia , Adolescente , Adulto , Boston/epidemiologia , Criança , Pré-Escolar , Terapia Combinada , Feminino , Síndrome de Goldenhar/epidemiologia , Humanos , Lactente , Recém-Nascido , Londres/epidemiologia , Masculino , Países Baixos/epidemiologia , Estudos Retrospectivos , Índice de Gravidade de Doença , Apneia Obstrutiva do Sono/epidemiologia , Resultado do Tratamento
8.
Br J Dermatol ; 176(5): 1131-1143, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28078671

RESUMO

Congenital melanocytic naevi (CMN) are a known risk factor for melanoma, with the greatest risk currently thought to be in childhood. There has been controversy over the years about the incidence of melanoma, and therefore over the clinical management of CMN, due partly to the difficulties of histological diagnosis and partly to publishing bias towards cases of malignancy. Large cohort studies have demonstrated that melanoma risk in childhood is related to the severity of the congenital phenotype. New understanding of the genetics of CMN offers the possibility of improvement in diagnosis of melanoma, identification of those at highest risk, and new treatment options. We review the world literature and our centre's experience over the last 25 years, including the molecular characteristics of melanoma in these patients and new melanoma incidence and outcome data from our prospective cohort. Management strategies are proposed for presentation of suspected melanoma of the skin and the central nervous system in patients with CMN, including use of oral mitogen-activated protein kinase kinase inhibitors in NRAS-mutated tumours.


Assuntos
Neoplasias Encefálicas/etiologia , Melanoma/etiologia , Nevo Pigmentado/congênito , Neoplasias Cutâneas/etiologia , Criança , Pré-Escolar , Feminino , GTP Fosfo-Hidrolases/genética , Humanos , Lactente , Masculino , Melanoma/patologia , Melanoma/terapia , Proteínas de Membrana/genética , Quinases de Proteína Quinase Ativadas por Mitógeno/antagonistas & inibidores , Mosaicismo , Mutação/genética , Fatores de Risco , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/terapia
9.
Sci Rep ; 6: 24251, 2016 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-27080443

RESUMO

Expression of major histocompatibility antigens class-2 (MHC-II) under non-inflammatory conditions is not usually associated with the nervous system. Comparative analysis of immunogenicity of human embryonic/fetal brain-derived neural stem cells (hNSCs) and human mesenchymal stem cells with neurogenic potential from umbilical cord (UC-MSCs) and paediatric adipose tissue (ADSCs), while highlighting differences in their immunogenicity, led us to discover subsets of neural cells co-expressing the neural marker SOX2 and MHC-II antigen in vivo during human CNS development. MHC-II proteins in hNSCs are functional, and differently regulated upon differentiation along different lineages. Mimicking an inflammatory response using the inflammatory cytokine IFNγ induced MHC-II up-regulation in both astrocytes and hNSCs, but not in UC-MSCs and ADSCs, either undifferentiated or differentiated, though IFNγ receptor expression was comparable. Together, hypoimmunogenicity of both UC-MSCs and ADSCs supports their suitability for allogeneic therapy, while significant immunogenicity of hNSCs and their progeny may at least in part underlie negative effects reported in some patients following embryonic neural cell grafts. Crucially, we show for the first time that MHC-II expression in developing human brains is not restricted to microglia as previously suggested, but is present in discrete subsets of neural progenitors and appears to be regulated independently of inflammatory stimuli.


Assuntos
Diferenciação Celular/genética , Regulação da Expressão Gênica no Desenvolvimento , Antígenos de Histocompatibilidade Classe II/genética , Interferon gama/metabolismo , Células-Tronco Neurais/citologia , Células-Tronco Neurais/metabolismo , Tecido Adiposo/citologia , Astrócitos/citologia , Astrócitos/metabolismo , Biomarcadores , Sangue Fetal/citologia , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Antígenos de Histocompatibilidade Classe I/genética , Antígenos de Histocompatibilidade Classe I/imunologia , Antígenos de Histocompatibilidade Classe II/imunologia , Humanos , Interferon gama/farmacologia , Neurônios/citologia , Neurônios/metabolismo , Receptores de Interferon/metabolismo
10.
Br J Oral Maxillofac Surg ; 54(1): 51-6, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26608690

RESUMO

The surgical treatment of defects caused by noma is challenging for the surgeon and the patient. Local flaps are preferred, but sometimes, because of the nature of the disease, there is not enough local tissue available. We describe our experience of free tissue transfer in Ethiopia. Between 2008 and 2014, 34 microsurgical procedures were done over 11 missions with the charity Facing Africa, predominantly for the treatment of defects caused by noma (n=32). The mean duration of operation was 442 minutes (range 200 - 720). Six minor wound infections were treated conservatively and did not affect outcome, a return to theatre was required in 4 patients with wound infections and one with a haemorrhage; 2 flaps failed and 2 partially failed, one patient developed an oronasal fistula, and one had an infection at the donor site that required a repeat graft. In settings where resources are limited, free flaps can be used when local tissue is not available and they cause less morbidity than pedicled tissue transfer.


Assuntos
Face/cirurgia , Microvasos/cirurgia , Procedimentos de Cirurgia Plástica , Retalhos de Tecido Biológico/cirurgia , Humanos , Microcirurgia , Noma/cirurgia , Retalhos Cirúrgicos/cirurgia
11.
Open Orthop J ; 10: 849-861, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-28217210

RESUMO

BACKGROUND: Bone is the second most transplanted tissue and due to its complex structure, metabolic demands and various functions, current reconstructive options such as foreign body implants and autologous tissue transfer are limited in their ability to restore defects. Most tissue engineering approaches target osteoinduction of osteoprogenitor cells by modifying the extracellular environment, using scaffolds or targeting intracellular signaling mechanisms or commonly a combination of all of these. Whilst there is no consensus as to what is the optimal cell type or approach, nanotechnology has been proposed as a powerful tool to manipulate the biomolecular and physical environment to direct osteoprogenitor cells to induce bone formation. METHODS: Review of the published literature was undertaken to provide an overview of the use of nanotechnology to control osteoprogenitor differentiation and discuss the most recent developments, limitations and future directions. RESULTS: Nanotechnology can be used to stimulate osteoprogenitor differentiation in a variety of way. We have principally classified research into nanotechnology for bone tissue engineering as generating biomimetic scaffolds, a vector to deliver genes or growth factors to cells or to alter the biophysical environment. A number of studies have shown promising results with regards to directing ostroprogenitor cell differentiation although limitations include a lack of in vivo data and incomplete characterization of engineered bone. CONCLUSION: There is increasing evidence that nanotechnology can be used to direct the fate of osteoprogenitor and promote bone formation. Further analysis of the functional properties and long term survival in animal models is required to assess the maturity and clinical potential of this.

12.
Br J Oral Maxillofac Surg ; 53(10): 1001-6, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26520001

RESUMO

We describe a series of 8 patients who had total reconstruction of the nose during 4 separate missions to Ethiopia. The aetiology was noma (n=3), assault (n=2), acid burn (n=1), squamous cell carcinoma (n=1), and a sequela of meningococcal septicaemia (n=1). Reconstruction was with forehead flaps when adequate tissue was available (n=6) and with radial forearm flaps when it was not (n=2). Some reconstructive approaches require procedures to be done in stages, and in settings where resources are limited, difficulties with the continuity of care and provision for the management of complications, must be overcome.


Assuntos
Nariz/cirurgia , Procedimentos de Cirurgia Plástica , Humanos , Noma/cirurgia , Neoplasias Nasais/cirurgia , Retalhos Cirúrgicos/cirurgia
13.
Stem Cell Res ; 15(1): 1-13, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25957945

RESUMO

Human somatic stem cells with neural differentiation potential can be valuable for developing cell-based therapies, including treatment of birth-related defects, while avoiding issues associated with cell reprogramming. Precisely defining the "identity" and differentiation potential of somatic stem cells from different sources, has proven difficult, given differences in sets of specific markers, protocols used and lack of side-by-side characterization of these cells in different studies. Therefore, we set to compare expression of mesenchymal and neural markers in human umbilical cord-derived mesenchymal stem cells (UC-MSCs), pediatric adipose-derived stem cells (p-ADSCs) in parallel with human neural stem cells (NSCs). We show that UC-MSCs at a basal level express mesenchymal and so-called "neural" markers, similar to that we previously reported for the p-ADSCs. All somatic stem cell populations studied, independently from tissue and patient of origin, displayed a remarkably similar expression of surface markers, with the main difference being the restricted expression of CD133 and CD34 to NSCs. Expression of certain surface and neural markers was affected by the expansion medium used. As predicted, UC-MSCs and p-ADSCs demonstrated tri-mesenchymal lineage differentiation potential, though p-ADSCs display superior chondrogenic differentiation capability. UC-MSCs and p-ADSCs responded also to neurogenic induction by up-regulating neuronal markers, but crucially they appeared morphologically immature when compared with differentiated NSCs. This highlights the need for further investigation into the use of these cells for neural therapies. Crucially, this study demonstrates the lack of simple means to distinguish between different cell types and the effect of culture conditions on their phenotype, and indicates that a more extensive set of markers should be used for somatic stem cell characterization, especially when developing therapeutic approaches.


Assuntos
Diferenciação Celular , Células-Tronco/citologia , Tecido Adiposo/citologia , Biomarcadores/metabolismo , Linhagem da Célula , Citometria de Fluxo , Humanos , Células-Tronco Mesenquimais , Células-Tronco Neurais/citologia , Neurogênese , Neurônios/citologia , Fenótipo , Células-Tronco Pluripotentes/citologia , Células-Tronco/metabolismo , Cordão Umbilical/citologia
15.
J Plast Reconstr Aesthet Surg ; 67(5): 725-8, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24333233

RESUMO

Postpneumonectomy syndrome (PPS) is a rare syndrome whereby the airway and oesophagus become obstructed due to extreme rotation of the mediastinum after pneumonectomy. Our treatment of this condition involved mediastinal repositioning and placement of a saline filled tissue expander into the pleural space. This has not been reported in the plastic surgical literature and we describe technical difficulties and how they were overcome.


Assuntos
Obstrução das Vias Respiratórias/cirurgia , Doenças do Esôfago/cirurgia , Pneumonectomia/efeitos adversos , Implantação de Prótese/métodos , Dispositivos para Expansão de Tecidos , Obstrução das Vias Respiratórias/etiologia , Criança , Doenças do Esôfago/etiologia , Feminino , Humanos , Síndrome
16.
J Plast Reconstr Aesthet Surg ; 66(11): 1487-93, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23938195

RESUMO

INTRODUCTION: Autologous microtia reconstruction is generally performed in two stages. The second stage presents a unique opportunity to carry out other complementary procedures. The present study describes our approach to microtia reconstruction, wherein the second stage of reconstruction is combined with final refinements to the ear construct and/or additional procedures to enhance facial contour and symmetry. METHODS: Retrospective analysis of patients who underwent two-stage microtia reconstruction by a single surgeon (NWB) was conducted in order to ascertain those that had ancillary procedures at the time of the second stage. Patient and operative details were collected. RESULTS: Thirty-four patients (male, 15, median age and age range at second stage, 11 and 10-18 years, respectively) who had complementary procedures executed during the second stage of auricular reconstruction were identified. Collectively, these included centralizing genioplasty (n = 1), fat transfer (n = 22), ear piercing (n = 7), and contralateral prominauris correction (n = 7). Six patients had correction for unilateral isolated microtia and in the remaining 28 patients, auricular reconstruction for microtia associated with a named syndrome. All patients reported a high rate of satisfaction with the result achieved and the majority (85%) reported no perceived need for additional surgical refinements to the ear or procedure(s) to achieve further facial symmetry. No peri- or post-operative complications were noted. CONCLUSION: Combining the final stage of autologous microtia reconstruction with other ancillary procedures affords a superior aesthetic outcome and decreased patient morbidity.


Assuntos
Anormalidades Congênitas/cirurgia , Anormalidades Craniofaciais/cirurgia , Pavilhão Auricular/cirurgia , Orelha/anormalidades , Assimetria Facial/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Tecido Adiposo/transplante , Adolescente , Piercing Corporal , Criança , Microtia Congênita , Orelha/cirurgia , Pavilhão Auricular/anormalidades , Assimetria Facial/congênito , Feminino , Mentoplastia , Humanos , Masculino , Satisfação do Paciente , Procedimentos de Cirurgia Plástica/efeitos adversos , Estudos Retrospectivos
19.
J Hand Surg Eur Vol ; 32(6): 684-93, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17993432

RESUMO

Five cases of Wassel types III, IV and VII thumb duplication underwent a Bilhaut-Cloquet procedure. A stable and mobile metacarpophalangeal joint was achieved in all cases. Interphalangeal joint motion was limited but this joint was stable in all cases. The nail ridge in these thumbs was minimal. A strong, stable thumb of normal size and good appearance can result from the Bilhaut-Cloquet procedure. When one nail is 70% of normal width, a modified procedure using the whole of one nail will avoid the nail ridge, but the nail will still differ from normal.


Assuntos
Deformidades Congênitas da Mão/cirurgia , Osteotomia/métodos , Polegar/anormalidades , Polegar/cirurgia , Fios Ortopédicos , Pré-Escolar , Feminino , Articulações dos Dedos/fisiopatologia , Deformidades Congênitas da Mão/diagnóstico por imagem , Deformidades Congênitas da Mão/fisiopatologia , Humanos , Lactente , Masculino , Articulação Metacarpofalângica/fisiopatologia , Unhas , Radiografia , Amplitude de Movimento Articular/fisiologia , Instrumentos Cirúrgicos , Polegar/diagnóstico por imagem , Polegar/fisiopatologia , Cicatrização/fisiologia
20.
J Plast Reconstr Aesthet Surg ; 59(2): 130-6, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16703856

RESUMO

The use of tensor fasciae latae was first described as a rotation or island flap and evolved into a free flap in the late 1970s. This series of 85 patients undergoing free tensor fasciae latae transfer includes complex head and neck, abdominal wall and lower limb reconstruction. The overall success rate was 93% (79 patients), partial flap loss, 5% (four cases), and flap failure, 2% (two patients). Twelve patients (14%) required unplanned return to theatre for exploration resulting in a 75% salvage rate. We believe this series demonstrates the great versatility of this flap and highlights particular indications for its use.


Assuntos
Neoplasias de Cabeça e Pescoço/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Retalhos Cirúrgicos , Parede Abdominal/cirurgia , Adulto , Idoso , Idoso de 80 Anos ou mais , Fascia Lata/transplante , Feminino , Rejeição de Enxerto , Humanos , Traumatismos da Perna/cirurgia , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Reoperação , Transplante de Pele/métodos
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